作者:Andrea Pinto、Paola Conti、Lucia Tamborini、Carlo De Micheli
DOI:10.1016/j.tetasy.2009.02.010
日期:2009.3
This report describes an efficient synthesis of the natural isomer of acivicin, which is the only one provided with a noteworthy biological activity. The present procedure allowed the synthesis of (+)-1 in just five steps with a 34% overall yield. Due to the easy separation of the two diastereomers and to the availability of the starting material at low cost, the present procedure can be scaled-up to gram quantities. (c) 2009 Elsevier Ltd. All rights reserved.
PRODRUGS OF GLUTAMINE ANALOGS
申请人:The Johns Hopkins University
公开号:US20200230111A1
公开(公告)日:2020-07-23
Prodrugs of glutamine analogs, such as prodrugs of acivicin, are disclosed.